Combined natural killer cell and dendritic cell functional deficiency in KARAP/DAP12 loss-of-function mutant mice

被引:146
作者
Tomasello, E
Desmoulins, PO
Chemin, K
Guia, S
Cremer, H
Ortaldo, J
Love, P
Kaiserlian, D [1 ]
Vivier, E
机构
[1] INSERM, U404, Lyon 07, France
[2] CNRS Marseille Luminy, INSERM, Ctr Immunol, F-13288 Marseille 09, France
[3] Lab Genet & Physiol Dev, Marseille 09, France
[4] NCI, Expt Immunol Lab, DBS, FCRDC, Frederick, MD 21702 USA
[5] NICHD, Sect Cellular & Dev Biol, Lab Mammalian Genes & Dev, NIH, Bethesda, MD 20892 USA
[6] Inst Univ France, Paris, France
关键词
D O I
10.1016/S1074-7613(00)00035-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
KARAP/DAP12 is a transmembrane polypeptide with an intracytoplasmic immunoreceptor tyrosine-based activation motif (ITAM). KARAP/DAP12 is associated with several activating cell surface receptors in hematopoietic cells. Here, we report that knockin mice bearing a nonfunctional KARAP/DAP12 ITAM present altered innate immune responses. Although in these mice NK cells are present and their repertoire of inhibitory MHC class I receptors is intact, the NK cell spectrum of natural cytotoxicity toward tumor cell targets is restricted. KARAP/DAP12 loss-of-function mutant mice also exhibit a dramatic accumulation of dendritic cells in muco-cutaneous epithelia, associated with an impaired hapten-specific contact sensitivity. Thus, despite its homology with CD3 zeta and FcR gamma, KARAP/DAP12 plays a specific role in innate immunity, emphasizing the nonredundancy of these ITAM-bearing polypeptides in hematopoietic cells.
引用
收藏
页码:355 / 364
页数:10
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